NM_001387889.1(SFMBT2):c.2146G>A (p.Gly716Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004191250.1
Allele description [Variation Report for NM_001387889.1(SFMBT2):c.2146G>A (p.Gly716Arg)]
NM_001387889.1(SFMBT2):c.2146G>A (p.Gly716Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 7, 2024